Comparing Tissue Adhesives in Port Site Closure

Description

This is a multi-center randomized controlled trial to evaluate two different methods of reinforcing surgical port site closure: 2-Octylcyanoacrylate and n-butyl-2-cyanoacrylate.

Conditions

Dermatitis, Contact

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Study Overview

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Study Details

Study overview

This is a multi-center randomized controlled trial to evaluate two different methods of reinforcing surgical port site closure: 2-Octylcyanoacrylate and n-butyl-2-cyanoacrylate.

Comparing Tissue Adhesives in Port Site Closure: A Randomized Controlled Trial

Comparing Tissue Adhesives in Port Site Closure

Condition
Dermatitis, Contact
Intervention / Treatment

-

Contacts and Locations

Houston

Memorial Hermann, Houston, Texas, United States, 77030

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 18 or older
  • * undergoing an elective laparoscopic or robotic abdominal surgery
  • * Patients unlikely to follow-up (live out of state, unable to be reached by phone or email)
  • * Patients with a known allergy to 2-Octylcyanoacrylate or N-butyl-2-cyanoacrylate.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

The University of Texas Health Science Center, Houston,

Study Record Dates

2025-10-29